218 related articles for article (PubMed ID: 3836314)
1. A 14-year-old girl with Turner syndrome of complicated karyotype; 45,X/47,XY,+18,-19,+der(19),t(Y;19)(q12;p13.3).
Niihira S; Fujita H; Otzuka N; Hashimoto T; Nagano M; Kondou T
Jinrui Idengaku Zasshi; 1985 Dec; 30(4):307-11. PubMed ID: 3836314
[No Abstract] [Full Text] [Related]
2. Turner syndrome and 45,X/47,XXX mosaicism.
Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
[TBL] [Abstract][Full Text] [Related]
3. Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
Gole LA; Lim J; Crolla JA; Loke KY
Singapore Med J; 2008 Apr; 49(4):349-51. PubMed ID: 18418530
[TBL] [Abstract][Full Text] [Related]
4. Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism.
Fryns JP; Pedersen JC; Goddeeris P; van den Berghe H
Ann Genet; 1980; 23(1):54-6. PubMed ID: 6965844
[No Abstract] [Full Text] [Related]
5. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
[TBL] [Abstract][Full Text] [Related]
6. [45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome].
Gil R; Galán F; López-Ginés C; Gregori-Romero M; Millet A; Pellín A; Llombart-Bosch A
Rev Clin Esp; 1991 Jun; 189(1):23-5. PubMed ID: 1924922
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic spectrum of 45,X/46,XY individuals.
Rosenberg C; Frota-Pessoa O; Vianna-Morgante AM; Chu TH
Am J Med Genet; 1987 Jul; 27(3):553-9. PubMed ID: 3631129
[TBL] [Abstract][Full Text] [Related]
8. [Sexual ambiguity and non-fluorescent Y chromosome in 45,X/46,XY mosaicism].
Lukusa T; Fryns JP; Vereecken R; Van den Berghe H
Arch Fr Pediatr; 1986 Apr; 43(4):263-5. PubMed ID: 3767589
[TBL] [Abstract][Full Text] [Related]
9. [Asymmetric mixed gonadal dysgenesis (author's transl)].
Glatzl J; Müller W; Zierler H; Rosenkranz W
Padiatr Padol; 1981; 16(2):195-201. PubMed ID: 7243331
[TBL] [Abstract][Full Text] [Related]
10. Presence of H-Y antigen in female patients with sex-chromosome mosaics and absence of testicular tissue.
Müller U; Mayerova A; Fraccaro M; Zuffardi O; Mikkelsen M; Prader A
Am J Med Genet; 1983 Jun; 15(2):315-21. PubMed ID: 6603793
[TBL] [Abstract][Full Text] [Related]
11. [DNA content and the size of Y chromosome in a patient with mixed gonadal dysgenesis and 45,X/46,Xt(Y:Y) (pter leads to q12::q12 leads to q11) karyotype].
Parcheta B; Skawiński W; Wiśniewski L
Ginekol Pol; 1982 Dec; 53(12):889-95. PubMed ID: 6892216
[No Abstract] [Full Text] [Related]
12. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
Canún S; Mutchinick O; Shaffer LG; Fernández C
Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
[TBL] [Abstract][Full Text] [Related]
13. The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants.
Nishi MY; Costa EM; Oliveira SB; Mendonca BB; Domenice S
Horm Res Paediatr; 2011; 75(1):26-31. PubMed ID: 20699606
[TBL] [Abstract][Full Text] [Related]
14. 45,X/46,XY mosaicism. A clinical review and report of ten cases.
Knudtzon J; Aarskog D
Eur J Pediatr; 1987 May; 146(3):266-71. PubMed ID: 3595646
[TBL] [Abstract][Full Text] [Related]
15. Germ cell tumor showing partial trisomy 1 in a gonadectomized intersex child with monosomy X and double Y mosaicism.
Ogur G; Pinarli FG; Dağdemir A; Artan S; Artürk E; Elli M; Sezer OT; Okten G
J Pediatr Hematol Oncol; 2006 Nov; 28(11):750-4. PubMed ID: 17114963
[TBL] [Abstract][Full Text] [Related]
16. [Asymmetrical gonadal dysgenesis. Report of a case (author's transl)].
Chapoy P; Mattei JF; Exbrayat C; Louchet E
Ann Genet; 1979; 22(3):173-7. PubMed ID: 316676
[TBL] [Abstract][Full Text] [Related]
17. Discordant phenotypes and 45,X/46,X,idic(Y).
Kelly TE; Franko JB; Rogol A; Golden WL
J Med Genet; 1998 Oct; 35(10):862-4. PubMed ID: 9783714
[TBL] [Abstract][Full Text] [Related]
18. Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants.
dos Santos AP; Andrade JG; Piveta CS; de Paulo J; Guerra G; de Mello MP; Maciel-Guerra AT
BMC Med Genet; 2013 Nov; 14():115. PubMed ID: 24192396
[TBL] [Abstract][Full Text] [Related]
19. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
Bergendi E; Plöchl E; Vlasak I; Rittinger O; Muss W
Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
[TBL] [Abstract][Full Text] [Related]
20. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA
Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]